The Mutation P.T613a in the Pore Helix of the Kv11.1 Potassium Channel is Associated with Long QT Syndrome

Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencing

(2014) James R. Priest et al.   HEART RHYTHM

MutationTaster2: mutation prediction for the deep-sequencing age

(2014) Jana Marie Schwarz et al.   NATURE METHODS

Cardiac Potassium Channel Subtypes: New Roles in Repolarization and Arrhythmia

(2014) Nicole Schmitt et al.   PHYSIOLOGICAL REVIEWS

Open conformation of hERG channel turrets revealed by a specific scorpion toxin BmKKx2

(2014) You-Tian Hu et al.   Cell and Bioscience

A novel mutation in the KCNH2 gene associated with short QT syndrome

(2010) Yaxun Sun et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

The genetic basis of long QT and short QT syndromes: A mutation update

(2009) Paula L. Hedley et al.   HUMAN MUTATION

Genotype-Phenotype Aspects of Type 2 Long QT Syndrome

(2009) Wataru Shimizu et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY